A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17456159



Internal ID22514036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102804610..102807138hg38UCSC Ensembl
chr10:104564367..104566895hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg382529
hg192529
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5863029
Supporting Variants
Samples
Known GenesWBP1L
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17456159
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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